860858001: Glycogen storage disease due to muscle pyruvate kinase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease due to muscle pyruvate kinase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease due to muscle pyruvate kinase deficiency
• \Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen storage disease due to muscle pyruvate kinase deficiency
• \Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease due to muscle pyruvate kinase deficiency

Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3944365014	Glycogen storage disease due to muscle pyruvate kinase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3944366010	Glycogen storage disease due to muscle pyruvate kinase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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